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趋化因子在恶性肿瘤中的多方面作用。

The multifaceted roles of chemokines in malignancy.

作者信息

Ben-Baruch A

机构信息

Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.

出版信息

Cancer Metastasis Rev. 2006 Sep;25(3):357-71. doi: 10.1007/s10555-006-9003-5.

Abstract

Tumor development and progression are multifactorial processes, regulated by a large variety of intrinsic and microenvironmental factors. A key role in cancer is played by members of the chemokine superfamily. Chemokines and their receptors are expressed by tumor cells and by host cells, in primary tumors and in specific metastatic loci. The effects of chemokines on tumorigenesis are diverse: While some members of the superfamily significantly support this process, others inhibit fundamental events required for tumor establishment and metastasis. The current review describes the multifaceted roles of chemokines in malignancy, addressing four major aspects of their activities: (1) inducing leukocyte infiltration to tumors and regulating immune functions, with emphasis on tumor-associated macrophages (and the chemokines CCL2, CCL5), T cells (and the chemokines CXCL9, CXCL10) and dendritic cells (and the chemokines CCL19, CCL20, CCL21); (2) directing the homing of tumor cells to specific metastatic sites (the CXCL12-CXCR4 axis); (3) regulating angiogenic processes (mainly the ELR(+)-CXC and non-ELR-CXC chemokines); (4) acting directly on the tumor cells to control their malignancy-related functions. Together, these different chemokine functions establish a net of interactions between the tumor cells and their microenvironment, and partly dictate the fate of the malignancy cascade.

摘要

肿瘤的发生和进展是多因素过程,受多种内在和微环境因素调控。趋化因子超家族成员在癌症中发挥关键作用。趋化因子及其受体在肿瘤细胞和宿主细胞中表达,存在于原发性肿瘤和特定转移位点。趋化因子对肿瘤发生的影响是多样的:超家族的一些成员显著促进这一过程,而其他成员则抑制肿瘤形成和转移所需的基本事件。本综述描述了趋化因子在恶性肿瘤中的多方面作用,涉及它们活动的四个主要方面:(1)诱导白细胞浸润至肿瘤并调节免疫功能,重点是肿瘤相关巨噬细胞(以及趋化因子CCL2、CCL5)、T细胞(以及趋化因子CXCL9、CXCL10)和树突状细胞(以及趋化因子CCL19、CCL20、CCL21);(2)引导肿瘤细胞归巢至特定转移部位(CXCL12 - CXCR4轴);(3)调节血管生成过程(主要是ELR(+) - CXC和非ELR - CXC趋化因子);(4)直接作用于肿瘤细胞以控制其与恶性肿瘤相关的功能。这些不同的趋化因子功能共同建立了肿瘤细胞与其微环境之间的相互作用网络,并部分决定了恶性肿瘤级联反应的命运。

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